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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376556Generated: October 29, 2026

Hydrochloric Acid → Ethanone, 2-chloro-1-(tetrahydro-2-furanyl)- (9CI)

https://huagongshe.com/reaction/376556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiazomethaneHCID 9550—
ReactantTetrahydro-2-furancarbonyl chlorideHCID 551254—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductEthanone, 2-chloro-1-(tetrahydro-2-furanyl)- (9CI)HCID 1039697441%

Reaction Steps

Oxalyl chloride (5.2ml, 60mmol) and DMF (1 drop) were added to (RS)-2-tetrahydrofuroic acid (W. E. Kaufmann and R. Adams, J.Amer.Chem.Soc., 1923, 45, 3029) (4.64g, 40mmol) in dichloromethane (25ml). The mixture was stirred 1h, evaporated in vacuo, dichloromethane added and reevaporated to give 2-tetrahydrofuroyl chloride, vmax (CH2Cl2) 1795cm-1. 2-Tetrahydrofuroyl chloride in ether (25ml) and dichloromethane (10ml) was added dropwise to an ice bath cooled solution of diazomethane (ca 80mmol) in ether (150ml). The reaction mixture was stirred 0.25h then a stream of hydrogen chloride gas passed into the solution for ca 2 minutes then stirred a further 0.25h, washed with saturated brine, dried, concentrated and flash chromatographed on silica gel eluting with 5,7.5 and 10% ethyl acetate in hexane to provide the title compound (2.46g, 41%); (Found: M+, 148.0279. C6H ClO2 requires M, 148.0291); vmax (CH2Cl2) 1739, 1395, 1071 and 936cm-1 ; δH (CDCl3, 250MHz) 1.8-2.4 (4H, m) and 3.9-4.6 (5H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06020329
Source datasetuspto-grants-2000_02
ORD IDord-30c9f0b7974243fc903c4d6a8de89859
Source noteuspto-grants-2000_02